• 제목/요약/키워드: anthracene derivative

검색결과 13건 처리시간 0.021초

Synthesis of Porphyrin-Viologen-Anthracene Triad for Construction of Photoactive Pseudorotaxane with Bis(p-phenylene)crownether

  • Shin, Eun Ju
    • Rapid Communication in Photoscience
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    • 제2권2호
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    • pp.39-41
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    • 2013
  • It is interesting to introduce viologen moiety into photoactive compounds such as porphyrin and anthracene in the study of supramolecular system such as pseudorotaxanes. For the construction of photoactive pseudorotaxane based on porphyrin-viologen-anthracene triad or its zinc derivative threaded with bis-p-phenylene-34-crown-10 macrocycle, porphyrin-viologen-anthracene triad 1 and its zinc derivative zinc porphyrin-viologen-anthracene triad 2 were prepared and their absorption and fluorescence spectral properties were measured.

Efficient Blue Light Emitting Diode by Using Anthracene Derivative with 3,5-Diphenylphenyl Wings at 9- and 10-Position

  • Kim, Yun-Hi;Lee, Sung-Joong;Jung, Sang-Yun;Byeon, Ki-Nam;Kim, Jeong-Sik;Shin, Sung-Chul;Kwon, Soon-Ki
    • Bulletin of the Korean Chemical Society
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    • 제28권3호
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    • pp.443-446
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    • 2007
  • The novel blue light emitting material, 9,10-bis(3',5'-diphenylphenyl)anthracene (BDA) was synthesized by Suzuki coupling reaction and characterized by the measurements of 1H NMR, 13C NMR and FT-IR. The new anthracene derivative, which contains anthracene as a main core unit and 3',5'-diphenylphenyl group derivative as wings, has high fluorescence yield, good thermal stability, and high glass transition temperature at 188 oC. With the newly non-doped blue emitting material in the multilayer device structure, it was possible to achieve the current efficiency of 3.0 cd/A. The EL spectrum of the ITO/CuPc/α-NPD/BDA/Alq3/LiF/Al device showed a maximum wavelength (λmax) at 440 nm. The emitting color of device showed the blue emission (x,y) = (0.18,0.19) at 10 mA/cm2 in CIE (Commission Internationale de l'Eclairage) chromaticity coordinates.

Synthesis and Electro-optic Properties of Anthracene Derivatives for Blue Emitting OLED Devices.

  • Park, Eun-Jung;Lyu, Eon-Joo;Kim, Soon-Hak;Kwak, Gi-Seop;Lee, Yun-Su;Park, Lee-Soon
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2007년도 7th International Meeting on Information Display 제7권1호
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    • pp.651-654
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    • 2007
  • Anthracene derivatives, 9,10trimethylsilylanthr - acene(SA) and bis(2-phenylethynyl)trimethylsilyl anthracene(Si-BPEA) were synthesized and their emission properties were studied with UV and PL spectrometers. The PL maxima of anthracene, SA, bis(2-phenylethynyl)anthracene (BPEA), Si-BPEA were obtained at 401, 438, 475, 478nm, respectively. The electro-optical properties OLED devices made with these anthracene derivatives were discussed.

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Fluorescent White OLEDs with a High Color-rendering Index Using a Silicon-Cored Anthracene Derivative as a Blue Host

  • Kwak, Jeong-Hun;Lyu, Yi-Yeol;Lee, Hyun-Koo;Char, Kook-Heon;Lee, Chang-Hee
    • Journal of Information Display
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    • 제11권3호
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    • pp.123-127
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    • 2010
  • Fluorescent white organic light-emitting diodes showing high color-rendering indices (CRIs) of up to 81 was demonstrated, with a silicon-cored anthracene derivative (PATSPA) doped with DPAVBi utilized as the deep-blue host and dye materials, and the commercial dyes rubrene and DCM2 utilized as the orange- and red-light-emitting dyes. The devices, consisting of three emissive layers, showed bright-white-light emission, but the ratio of the blue peak to the orange and red peaks changed with the current density and the thickness of the blue emissive layer. A high CRI was achieved with the use of a deep-blue emitter doped in a novel host and by optimizing the blue-layer thickness. The device with a blue-layer thickness of 10 nm showed the Commission Internationale de l'Eclairage (CIE) color coordinate of (0.33, 0.35), a high CRI of 81, and a moderate external quantum efficiency of 2% at a current density of $2.5\;mA/cm^2$.

부피가 큰 치환체를 포함하는 카바졸과 결합한 안트라센 화합물의 합성 (Synthesis of Anthracene Derivative Combined with Cabazole Containing Bulky Substituent)

  • 안상원;윤구영;이승희
    • 한국응용과학기술학회지
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    • 제30권1호
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    • pp.160-165
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    • 2013
  • 유기전기발광 소자에서 천연색을 구현하기 위해서는 적색, 녹색, 청색 발광물질이 필요하다. 그러나 적색과 녹색의 발광 물질에 대한 연구는 매우 활발하나 청색의 물질에 대한 연구가 미흡한 것은 높은 발광 에너지 때문으로 보인다. 본 연구는 발광 효율이 높으며 열적 안정성이 좋은 화합물을 합성하려는 것으로 carbazole로 치환된 anthracene 화합물 합성에 관한 것이다. Tert-butyl 기로 치환된 carbazole에 전기 발광 성질과 열적 안정도가 좋은 anthracene을 직접 결합시킴으로써 정공전달 특성을 갖는 작용기와 전자전달 특성을 갖는 작용기 간의 거리에 대한 연구를 시작하고자 하였다.

Color Pure and Stable Blue Light Emitting Material Containing Anthracene and Fluorene for OLED

  • Park, Hyun-Tae;Oh, Dae-Hwan;Park, Jong-Won;Kim, Jin-Hak;Shin, Sung-Chul;Kim, Yun-Hi;Kwon, Soon-Ki
    • Bulletin of the Korean Chemical Society
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    • 제31권7호
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    • pp.1951-1955
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    • 2010
  • A new blue light emitting anthracene derivative, 9,10-bis-(9',9'-diethyl-7'-t-butyl-fluoren-2'-yl)anthracene (BETF), has been designed and synthesized by a palladium catalyzed Suzuki cross-coupling. A theoretical calculation of the three-dimensional structure of BETF supports that it has a non coplanar structure and inhibited intermolecular interactions resulting in high luminescent efficiency and high color purity. BETF has good thermal stability with glass-transition temperature (Tg) of $131^{\circ}C$. The PL maximum of BETF in solution and film were 438 nm and 440 nm, respectively, showing pure blue emission. A multilayer device using BETF as emitting material exhibits maximum luminescence efficiency of 2.2 cd/A and a pure blue emission (Commission Internationale de L'Eclairage (CIE) coordinates of x = 0.15, y = 0.10).

Photoelectron Transport Across Phospholipid Liposomes Pigmented by Anthracene and Naphthalene Derivatives

  • Lee, Yong-Ill;Kwon, Hwang-Won;Shin, Dae-Hyon;Yoon, Min-Joong
    • Bulletin of the Korean Chemical Society
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    • 제7권2호
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    • pp.120-124
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    • 1986
  • In order to investigate effective solar energy conversion system, the light-induced electron transfer reactions have been examined across single-lamellar liposomes incorporated organic photosensitizers such as anthracene and naphthalene derivatives. We have observed photosensitized reduction of methyl viologen (1,1'-dimethyl-4,4'-$bipyridinium^{2+}$) dissolved in the exterior aqueous phase of the pigmented phospholipid liposomes when EDTA, as electron donor, is dissolved in the enclosed aqueous phase of the liposomes. The anthroyl stearic acid incorporated in the hydrophobic bilayer of liposomes leads to much less quantum yield for the photosensitized reduction of $MV^{2+}$ than the anthracene carboxylate incorporated in the outer hydrophilic layer. However, ${\beta}$-carotene with anthroyl stearic acid incorporated into the bilayer enhances the quantum yield significantly (${\Phi}{\simeq}0.2-0.3$), preventing the reverse reaction of electron transfer ($MV^+_\ {\rightarrow}MV^{2+}$) so that it might be useful for solar energy conversion into chemical energy. A naphthalene derivative, octadecyl naphthylamine sulfonic acid incorporated into the outer layer of liposomes results in less efficiency of $MV^{2+}$ reduction than anthroyl stearic acid. These results have been also tested with respect to lipid components of liposomes.

이차 미분 형광 분광광도법에 의한 울산만 해양 저질토양 중의 다환 방향족 탄화수소(PAHs)의 동시 분석 (Synchronous determination of polycyclic aromatic hydrocarbons(PAHs) in sediment of Ulsan Bay by synchronous 2nd derivative fluorescence spectrophotometry)

  • 유광식;정지영;정선이
    • 분석과학
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    • 제17권1호
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    • pp.45-52
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    • 2004
  • 현이차 미분 형광 분광광도법을 이용하여 울산만 해양 저질토양중의 PAHs를 n-hexane용매로 추출하여 11종의 PAHs를 동시 정량분석하였다. Acenaphthene (Ace), anthracene (Anth), benzo(a)pyrene (BaP), benz(a)anthracene (BaA), benzo(b)fluoranthene (BbFt), benzo(k)fluoranthene (BkFt), chrysene (Chry), perylene (Per), phenanthrene (Phen), pyrene (Pyr) 및 fluoranthrene (Ft) 등을 정량분석 하였다. 이들 성분들의 검정선은 대략 0.15~166 ppb의 농도범위에서 직선관계를 보였으며, 0.999이상의 좋은 직선 상관계수를 보였다. 울산만의 해양 저질 토양 (sediment)에 함유된 11종의 PAHs 총량은 68.8 ng/g ~ 324.4 ng/g의 농도범위로 함유되어 있었다. 또한 PAHs의 총량은 울산만의 안쪽으로 갈수록 증가하는 경향을 보였으며, 특히 Pyr과 BaA 등과 같은 4고리화합물의 함량비가 높았다.

7, 12-dimethylbenz[a]anthracene(DMBA)로 유발된 햄스터 협낭암에서 chlorophylln의 암예방효과에 관한 실험적 연구 (AN EXPERIMENTAL STUDY ON THE CHEMOPREVENTIVE EFFECT OF CHLOROPHYLLIN IN HAMSTER CHEEK POUCH TUMOR INDUCED BY 7, 12-DIMETHYLBENZ[A]ANTHRACENE)

  • 윤규호
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제26권2호
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    • pp.137-145
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    • 2000
  • Carcinogenesis is a multi-stage process that generally consists of at least three steps; initiation, promotion, and progression. If one of these carcinogenic steps were suppressed or delayed, the cancer could be prevented. Cancer chemoprevention is defined to be inhibition or reversal of the carcinogenic process by the specific chemical agents and is a novel approach to cancer management alternative to conventional chemotherapy. Chlorophylln(CHL), a water-soluble derivative of chlorophyll, containing sodium and copper, has been known to be strong antimutagen in several test systems, but its mechanism of antimutagenic action is unknown. In the present experiment, the possibility of CHL as chemopreventive drugs on 7,12-dimethylbenz[a]anthracene(DMBA)-induced hamster buccal pouch carcinogenesis was investigated by mutagenicity test, carcinogenicity test, and frequency or spectrum of H-ras mutations in the both of DMBA-induced and chlorophylln-pretreated-DMBA induced tumor by polymerase chain reaction and non-isotopic restriction fragment length polymorphism. The treatment of CHL reduced the yields and multiplicity of the 0.5% DMBA-induced tumor, 86% to 62.5% and $3.7{\pm}0.6$ to $1.4{\pm}0.3$, respectively. The occurrence of histidine revertant by $20{\mu}mole$ DMBA was inhibited 25.6 to 81.7% by 1 to $5{\mu}M$ CHL in a dose-dependent manner. The mutation rates of H-ras gene in DMBA-induced and CHL-pretreated-DMBA induced tumor were 96%, 94% of which the most mutations were in codon 12/13. These results suggest that CHL inhibits the carcinogenic action of DMBA by the formation of complex between CHL and DMBA or the inhibition of the activation of DMBA in vivo. But CHL did not affect the mutation rates or its spectrum in already formed tumor.

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